| Literature DB >> 33202249 |
Kathrin Leppek1, Kotaro Fujii1, Nick Quade2, Teodorus Theo Susanto1, Daniel Boehringer2, Tea Lenarčič2, Shifeng Xue1, Naomi R Genuth1, Nenad Ban3, Maria Barna4.
Abstract
Ribosomes have been suggested to directly control gene regulation, but regulatory roles for ribosomal RNA (rRNA) remain largely unexplored. Expansion segments (ESs) consist of multitudes of tentacle-like rRNA structures extending from the core ribosome in eukaryotes. ESs are remarkably variable in sequence and size across eukaryotic evolution with largely unknown functions. In characterizing ribosome binding to a regulatory element within a Homeobox (Hox) 5' UTR, we identify a modular stem-loop within this element that binds to a single ES, ES9S. Engineering chimeric, "humanized" yeast ribosomes for ES9S reveals that an evolutionary change in the sequence of ES9S endows species-specific binding of Hoxa9 mRNA to the ribosome. Genome editing to site-specifically disrupt the Hoxa9-ES9S interaction demonstrates the functional importance for such selective mRNA-rRNA binding in translation control. Together, these studies unravel unexpected gene regulation directly mediated by rRNA and how ribosome evolution drives translation of critical developmental regulators.Entities:
Keywords: ES9S; Hox cluster; RNA structure; RNA-protein interaction; expansion segment; internal initiation; internal ribosome entry site; mRNA translation; ribosomal RNA; ribosome; ribosome engineering; stem-loop; yeast
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Year: 2020 PMID: 33202249 PMCID: PMC7769145 DOI: 10.1016/j.molcel.2020.10.023
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970